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骨骼肌毛细血管密度:II-III级慢性心力衰竭运动不耐受的一种促成机制,独立于其他外周改变。

Capillary density of skeletal muscle: a contributing mechanism for exercise intolerance in class II-III chronic heart failure independent of other peripheral alterations.

作者信息

Duscha B D, Kraus W E, Keteyian S J, Sullivan M J, Green H J, Schachat F H, Pippen A M, Brawner C A, Blank J M, Annex B H

机构信息

Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

J Am Coll Cardiol. 1999 Jun;33(7):1956-63. doi: 10.1016/s0735-1097(99)00101-1.

Abstract

OBJECTIVES

The study was conducted to determine if the capillary density of skeletal muscle is a potential contributor to exercise intolerance in class II-III chronic heart failure (CHF).

BACKGROUND

Previous studies suggest that abnormalities in skeletal muscle histology, contractile protein content and enzymology contribute to exercise intolerance in CHF.

METHODS

The present study examined skeletal muscle biopsies from 22 male patients with CHF compared with 10 age-matched normal male control patients. Aerobic capacities, myosin heavy chain (MHC) isoforms, enzymes, and capillary density were measured.

RESULTS

The patients with CHF demonstrated a reduced peak oxygen consumption when compared to controls (15.0+/-2.5 vs. 19.8+/-5.0 ml x kg(-1) x min(-1), p <0.05). Using cell-specific antibodies to directly assess vascular density, there was a reduction in capillary density in CHF measured as the number of endothelial cells/fiber (1.42+/-0.28 vs. 1.74+/-0.35, p = 0.02). In CHF, capillary density was inversely related to maximal oxygen consumption (r = 0.479, p = 0.02). The MHC IIx isoform was found to be higher in patients with CHF versus normal subjects (28.5+/-13.6 vs. 19.5+/-9.4, p <0.05).

CONCLUSIONS

There was a significant reduction in microvascular density in patients with CHF compared with the control group, without major differences in other usual histologic and biochemical aerobic markers. The inverse relationship with peak oxygen consumption seen in the CHF group suggests that a reduction in microvascular density of skeletal muscle may precede other skeletal muscle alterations and play a critical role in the exercise intolerance characteristic of patients with CHF.

摘要

目的

本研究旨在确定骨骼肌的毛细血管密度是否是导致Ⅱ-Ⅲ级慢性心力衰竭(CHF)患者运动不耐受的潜在因素。

背景

先前的研究表明,骨骼肌组织学、收缩蛋白含量和酶学异常是导致CHF患者运动不耐受的原因。

方法

本研究检查了22例男性CHF患者的骨骼肌活检样本,并与10例年龄匹配的正常男性对照患者进行比较。测量了有氧运动能力、肌球蛋白重链(MHC)亚型、酶和毛细血管密度。

结果

与对照组相比,CHF患者的峰值耗氧量降低(15.0±2.5 vs. 19.8±5.0 ml·kg⁻¹·min⁻¹,p<0.05)。使用细胞特异性抗体直接评估血管密度,CHF患者的毛细血管密度降低,以每根纤维的内皮细胞数量计算(1.42±0.28 vs. 1.74±0.35,p = 0.02)。在CHF患者中,毛细血管密度与最大耗氧量呈负相关(r = 0.479,p = 0.02)。发现CHF患者的MHC IIx亚型高于正常受试者(28.5±13.6 vs. 19.5±9.4,p<0.05)。

结论

与对照组相比,CHF患者的微血管密度显著降低,而其他常见的组织学和生化有氧运动标志物无明显差异。CHF组中观察到的与峰值耗氧量的负相关关系表明,骨骼肌微血管密度的降低可能先于其他骨骼肌改变,并在CHF患者运动不耐受的特征中起关键作用。

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